NM_007286.6(SYNPO):c.1505C>T (p.Thr502Met) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 7, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004246556.1
Allele description [Variation Report for NM_007286.6(SYNPO):c.1505C>T (p.Thr502Met)]
NM_007286.6(SYNPO):c.1505C>T (p.Thr502Met)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 1, 2024